Evidence map›Paper›PMID 30101091›Full record

ArticleVeterinary medicine (Auckland, N.Z.)2015

Feasibility of flotation concentration of fungal spores as a method to identify toxigenic mushrooms.

Lisa J Bazzle, Marc A Cubeta, Steven L Marks, David C Dorman

Abstract read
In one paragraph

Article in Veterinary medicine (Auckland, N.Z.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Lisa J BazzleDepartment of Clinical Sciences, College of Veterinary Medicine.
Marc A CubetaDepartment of Plant Pathology, College of Agriculture and Life Sciences, Center for Integrated Fungal Research.
Steven L MarksDepartment of Clinical Sciences, College of Veterinary Medicine.
David C DormanDepartment of Molecular and Biomedical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA, david_dorman@ncsu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMushroom poisoning is a recurring and challenging problem in veterinary medicine. Diagnosis of mushroom exposure in animals is hampered by the lack of rapid diagnostic tests. Our study evaluated the feasibility of using flotation concentration and microscopic evaluation of spores for mushroom identification. Evaluation of this method in living animals exposed to toxigenic mushrooms is limited by ethical constraints; therefore, we relied upon the use of an in vitro model that mimics the oral and gastric phases of digestion.

methodsIn our study, mycologist-identified toxigenic (poisonous) and nontoxigenic fresh mushrooms were collected in North Carolina, USA. In phase 1, quantitative spore recovery rates were determined following magnesium sulfate, modified Sheather's sugar solution, and zinc sulfate flotation (n=16 fungal species). In phase 2, mushrooms (n=40 fungal species) were macerated and digested for up to 2 hours in a salivary and gastric juice simulant. The partially digested material was acid neutralized, filtered, and spores concentrated using zinc sulfate flotation followed by microscopic evaluation of spore morphology.

resultsMean spore recovery rates for the three flotation fluids ranged from 32.5% to 41.0% (

conclusionFlotation can concentrate mushroom spores; however, false negative results can occur. Spore morphology could not be used to differentiate species of mushroom-forming fungi since the spore shape and surface characteristics seen in the present study were often observed with multiple species of mushroom-forming fungi.

Indexed as

Amanita sppgastrointestinal contentsmushroom spore identificationmushroom toxicity

Identifiers

PMID30101091
PMCPMC6067785

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